August 2018 FDA Recall Drug by Mckesson Corporation
D-1172-2018 - Supterpotent Drug

This Class II drug recall was voluntarily initiated by Mckesson Corporation on August 14, 2018 for the product Drug. The FDA reported the reason for recall as supterpotent drug. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-1172-2018

Reason for Recall
Supterpotent Drug
Initiated
08-14-2018
Reported
09-12-2018
Quantity
1531 cartons

Recall Profile & Regulatory Data

Event ID About Event ID
Numerical designation assigned by FDA to a specific recall event.
80830
Classification About Classification
Relative degree of health hazard assigned by FDA.
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
Mckesson Corporation
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Product Type About Product Type
Broad category of product being recalled.
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
Nationwide within the United States
Termination Date About Termination Date
Date that FDA officially terminated the recall.
11-25-2020
Product Description About Product Description
Full technical description of the product.
Megestrol Acetate Oral Suspension, USP 400 mg/mL, 10 mL (10 mL UD cups in boxes of 20 cups), Rx Only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977 Dist. By: McKesson Packaging Services a business unit of McKesson Corporation 7101 Weddington Rd. Concord, NC 28027, NDC 63739-549-51

Batch or Lot Expiration Information

Lot# : 0116158 Exp. 4/30/19; 0113903, 0113902, 0113901, Exp. 8/31/18